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HRID 3041생성일: 2026년 10월 23일

Acetic Acid → 4-(4-Acetamido-4-phenylpiperidino)-2-(3,4-dichlorophenyl)-N-[3,5-bis(trifluoromethyl)benzyl]butylamine

https://huagongshe.com/ko/reaction/3041

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-(4-Acetamido-4-phenylpiperidino)-2-(3,4-dichlorophenyl)butylamineHCID 19592198—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-(4-Acetamido-4-phenylpiperidino)-2-(3,4-dichlorophenyl)-N-[3,5-bis(trifluoromethyl)benzyl]butylamineHCID 57014931—

반응 조건

온도0 °C

반응 단계

To a solution of 4-(4-acetamido-4-phenylpiperidino)-2-(3,4-dichlorophenyl)butylamine (0.30 g) in methanol (3 mL) was added 3,5-bis(trifluoromethyl)benzaldehyde (0.088 mL) and the mixture cooled to 0° C. To this stirred mixture was sequentially added acetic acid (0.046 mL) and a solution of sodium cyanoborohydride (0.50 g) in methanol (1 mL). The mixture was allowed to slowly warm to room temperature overnight and was diluted with dichloromethane (5 mL), water (5 mL), and hydrochloric acid (1N, 5 mL). The layers were separated, and the aqueous layer was extracted three times with dichloromethane (10 mL). The acidic aqueous layer was made basic with aqueous sodium hydroxide (1N, 5 mL) and then extracted with 5:1 dichloromethane:methanol (3×10 mL). The combined organic layers were washed (brine), dried, filtered and evaporated to afford an oil which was purified by chromatography, with dichloromethane:methanol (40:1) as eluent. Evaporation of the appropriate fractions afforded a partial hydrate of the title compound as a white solid (0.154 g); mp 66°-68° C.; NMR: 7.82 (s,3), 7.75 (s,1), 7.50 (m,2), 7.35-5.15 (m,6), 2.75 (m,1), 2.65-2.55 (m,2), 2.32-1.95 (m,6), 1.85 (s,3), 1.95-1.55 (m,6); MS: m/z=660(M+1, 100%); Rf =0.51 (10:1, dichloromethane:methanol). Analysis for C32H33Cl2F6N3O.0.25 H2O: Calculated: C, 57.79; H, 5.08; N, 6.32; Found: C, 57.68; H, 5.07; N, 6.30.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731309
출처 데이터셋uspto-grants-1998_03
ORD IDord-7e4da2f6c23d4c1a8affe98a75ef0117
출처 메모uspto-grants-1998_03